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Related Concept Videos

RNA-seq03:21

RNA-seq

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
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The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
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CANEapp: a user-friendly application for automated next generation transcriptomic data analysis.

Dmitry Velmeshev1,2, Patrick Lally3,4, Marco Magistri5

  • 1Department of Psychiatry, University of Miami Miller School of Medicine, Miami, FL, 33136, USA. dvelmeshev@med.miami.edu.

BMC Genomics
|January 14, 2016
PubMed
Summary
This summary is machine-generated.

CANEapp simplifies complex next-generation sequencing data analysis with a user-friendly interface and automated pipeline, improving gene expression analysis and RNA discovery for researchers.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • Next-generation sequencing (NGS) generates large datasets, posing analysis challenges.
  • Complex computational skills (Linux, scripting) are often required for NGS data.
  • Efficient, validated analysis workflows are crucial for extracting biological insights.

Purpose of the Study:

  • To develop an automated, user-friendly tool for comprehensive next-generation sequencing (NGS) experiment analysis.
  • To address the computational bottleneck in NGS data analysis for researchers.
  • To provide a platform-independent solution for RNA-sequencing (RNA-seq) data.

Main Methods:

  • Developed CANEapp, a suite with a Graphical User Interface (GUI) and automated server-side pipeline.
  • Implemented automated installation of software and reference files on Linux servers.
  • Automated differential gene expression analysis and noncoding RNA discovery using Cuffdiff, edgeR, and DESeq2.

Main Results:

  • CANEapp offers a platform-independent GUI for RNA-seq analysis, connecting seamlessly to servers.
  • Automated workflows perform differential gene expression and noncoding RNA discovery.
  • CANEapp demonstrated improved performance over existing tools and was experimentally validated using qRT-PCR.

Conclusions:

  • CANEapp serves biologists and bioinformaticians, simplifying large RNA-seq dataset analysis.
  • The tool is accurate, powerful, and time-saving, facilitating future high-throughput genomics analysis.
  • Its standardized, automated, and platform-independent nature makes it ideal for collaborative projects.